Polyether polyols with increased functionality

a polyether polyol and functional technology, applied in the field of polyether polyols with increased functionality, can solve the problems of high explosiveness, process seriousness, and inapplicability, and achieve the effects of increasing the reactivity of isocyanates, increasing the functionality, and speeding up the reaction ra

Inactive Publication Date: 2003-06-26
BAYER POLYMERS LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

0050] In addition to exhibiting increased functionality over the starting epoxide-reactive compounds, the process of the present invention unexpectedly yielded polyether polyols with increased reactivity toward isocyanates. Polyether polyols prepared according to the invention exhibit a faster reaction rate than conventional polyether polyols. Since the reactivity of the resulting polyether polyols is higher, less catalyst is necessary in formulations to subsequently form polyurethanes from them.

Problems solved by technology

This is not practical since problems are caused in the handling of the high viscosity polyether polyol in normal foaming machines.
Also, there is a risk represented by handling large quantities of alkylene oxide within the reactors at the reaction temperature due to the high vapor pressure, which makes this highly explosive.
This process has some serious disadvantages, however.
First, the dispersing agents lower the reaction capacity by 10-40%.
Second, the dispersing agent must be removed at the end of the production process.
As is evident from the above, there is no method for the production of high functionality epoxide-reactive component based on cyanuric chloride.

Method used

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  • Polyether polyols with increased functionality
  • Polyether polyols with increased functionality
  • Polyether polyols with increased functionality

Examples

Experimental program
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Embodiment Construction

[0052] The following Table 1 illustrates the amount of material used in Example 1 which were reacted according to the invention to form the epoxide-reactive compound.

1 TABLE 1 Example 1 Amount Organic Compound A 300 g Cyanuric Chloride 21.5 g Solvent A: 50 mL

[0053] Organic Compound A: an organic compound started from glycerin, having a functionality of three (3), a molecular weight about of 480 and an OH number of about 351; and being prepared by reacting 1 mole of glycerin with 5 to 8 moles of PO (propylene oxide) and 7% by weight of KOH, and dewatering to give 5% by wt. potassium

[0054] Solvent A: N-methylpyrrolidinone

[0055] In Example 1 above, the cyanuric chloride was dissolved in Solvent A, thereby forming a solution. This solution was slowly added to Organic Compound A in the reaction vessel. The reaction mixture was heated to 100.degree. C. and maintained at this temperature for about 2 hours. The resulting material was filtered, and Solvent A was removed by distillation. This...

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Abstract

This invention relates to a process for the preparation an epoxide-reactive compound having a functionality of at least 3, a molecular weight of from about 250 to about 1,900, and an OH number of from about 85 to about 1,400. This process comprises reacting (a) an organic compound which is free of ether groups, having a molecular weight of from about 60 to about 600, and containing from about 2 to about 8 reactive sites; with (b) cyanuric chloride; optionally, in the presence of (c) one or more catalysts; wherein the functionality of the resultant epoxide-reactive compound equals three times the functionality of (a) said organic compound minus three. This invention also relates to further reacting the epoxide-reactive compound produced by the above process with an alkylene oxide, optionally in the presence of a catalyst to form a polyether polyol having a functionality of at least about 3, a molecular weight of from about 300 to about 18,000, and an OH number of from about 10 to about 565.

Description

[0001] This invention relates to a process for the preparation an epoxide-reactive compound having a functionality of at least 3, a molecular weight of from about 250 to about 1,900, and an OH number of from about 85 to about 1,400. This process comprises reacting (a) an organic compound which is free of ether groups, having a molecular weight of from about 60 to about 600, and containing from about 2 to about 8 reactive sites; with (b) cyanuric chloride; optionally, in the presence of (c) one or more catalysts; wherein the functionality of the resultant epoxide-reactive compound equals three times the functionality of (a) the organic compound minus three. This invention also relates to further reacting the epoxide-reactive compound produced by the above process with an alkylene oxide, optionally in the presence of a catalyst to form a polyether polyol having a functionality of at least about 3, a molecular weight of from about 300 to about 18,000, and an OH number of from about 10 ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C08G18/50C08G59/32
CPCC08G18/5063C08G2101/0025C08G59/3245C08G2110/0025
Inventor ADKINS, RICK L.PARSONS, HAROLD R.
Owner BAYER POLYMERS LLC
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